EP0762836B1 - Beverage compositions containing green tea solids, electrolytes and carbohydrates to provide improved cellular hydration and drinkability - Google Patents
Beverage compositions containing green tea solids, electrolytes and carbohydrates to provide improved cellular hydration and drinkability Download PDFInfo
- Publication number
- EP0762836B1 EP0762836B1 EP95919908A EP95919908A EP0762836B1 EP 0762836 B1 EP0762836 B1 EP 0762836B1 EP 95919908 A EP95919908 A EP 95919908A EP 95919908 A EP95919908 A EP 95919908A EP 0762836 B1 EP0762836 B1 EP 0762836B1
- Authority
- EP
- European Patent Office
- Prior art keywords
- beverage
- composition
- water
- electrolytes
- present
- Prior art date
- Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
- Expired - Lifetime
Links
Classifications
-
- A—HUMAN NECESSITIES
- A23—FOODS OR FOODSTUFFS; TREATMENT THEREOF, NOT COVERED BY OTHER CLASSES
- A23L—FOODS, FOODSTUFFS, OR NON-ALCOHOLIC BEVERAGES, NOT COVERED BY SUBCLASSES A21D OR A23B-A23J; THEIR PREPARATION OR TREATMENT, e.g. COOKING, MODIFICATION OF NUTRITIVE QUALITIES, PHYSICAL TREATMENT; PRESERVATION OF FOODS OR FOODSTUFFS, IN GENERAL
- A23L2/00—Non-alcoholic beverages; Dry compositions or concentrates therefor; Their preparation
- A23L2/52—Adding ingredients
-
- A—HUMAN NECESSITIES
- A23—FOODS OR FOODSTUFFS; TREATMENT THEREOF, NOT COVERED BY OTHER CLASSES
- A23F—COFFEE; TEA; THEIR SUBSTITUTES; MANUFACTURE, PREPARATION, OR INFUSION THEREOF
- A23F3/00—Tea; Tea substitutes; Preparations thereof
- A23F3/16—Tea extraction; Tea extracts; Treating tea extract; Making instant tea
- A23F3/163—Liquid or semi-liquid tea extract preparations, e.g. gels, liquid extracts in solid capsules
-
- A—HUMAN NECESSITIES
- A23—FOODS OR FOODSTUFFS; TREATMENT THEREOF, NOT COVERED BY OTHER CLASSES
- A23L—FOODS, FOODSTUFFS, OR NON-ALCOHOLIC BEVERAGES, NOT COVERED BY SUBCLASSES A21D OR A23B-A23J; THEIR PREPARATION OR TREATMENT, e.g. COOKING, MODIFICATION OF NUTRITIVE QUALITIES, PHYSICAL TREATMENT; PRESERVATION OF FOODS OR FOODSTUFFS, IN GENERAL
- A23L2/00—Non-alcoholic beverages; Dry compositions or concentrates therefor; Their preparation
- A23L2/38—Other non-alcoholic beverages
-
- A—HUMAN NECESSITIES
- A23—FOODS OR FOODSTUFFS; TREATMENT THEREOF, NOT COVERED BY OTHER CLASSES
- A23L—FOODS, FOODSTUFFS, OR NON-ALCOHOLIC BEVERAGES, NOT COVERED BY SUBCLASSES A21D OR A23B-A23J; THEIR PREPARATION OR TREATMENT, e.g. COOKING, MODIFICATION OF NUTRITIVE QUALITIES, PHYSICAL TREATMENT; PRESERVATION OF FOODS OR FOODSTUFFS, IN GENERAL
- A23L2/00—Non-alcoholic beverages; Dry compositions or concentrates therefor; Their preparation
- A23L2/385—Concentrates of non-alcoholic beverages
- A23L2/39—Dry compositions
- A23L2/395—Dry compositions in a particular shape or form
-
- A—HUMAN NECESSITIES
- A23—FOODS OR FOODSTUFFS; TREATMENT THEREOF, NOT COVERED BY OTHER CLASSES
- A23L—FOODS, FOODSTUFFS, OR NON-ALCOHOLIC BEVERAGES, NOT COVERED BY SUBCLASSES A21D OR A23B-A23J; THEIR PREPARATION OR TREATMENT, e.g. COOKING, MODIFICATION OF NUTRITIVE QUALITIES, PHYSICAL TREATMENT; PRESERVATION OF FOODS OR FOODSTUFFS, IN GENERAL
- A23L33/00—Modifying nutritive qualities of foods; Dietetic products; Preparation or treatment thereof
- A23L33/10—Modifying nutritive qualities of foods; Dietetic products; Preparation or treatment thereof using additives
- A23L33/16—Inorganic salts, minerals or trace elements
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
- A61K36/00—Medicinal preparations of undetermined constitution containing material from algae, lichens, fungi or plants, or derivatives thereof, e.g. traditional herbal medicines
- A61K36/18—Magnoliophyta (angiosperms)
- A61K36/185—Magnoliopsida (dicotyledons)
- A61K36/47—Euphorbiaceae (Spurge family), e.g. Ricinus (castorbean)
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
- A61K36/00—Medicinal preparations of undetermined constitution containing material from algae, lichens, fungi or plants, or derivatives thereof, e.g. traditional herbal medicines
- A61K36/18—Magnoliophyta (angiosperms)
- A61K36/185—Magnoliopsida (dicotyledons)
- A61K36/74—Rubiaceae (Madder family)
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
- A61K36/00—Medicinal preparations of undetermined constitution containing material from algae, lichens, fungi or plants, or derivatives thereof, e.g. traditional herbal medicines
- A61K36/18—Magnoliophyta (angiosperms)
- A61K36/185—Magnoliopsida (dicotyledons)
- A61K36/82—Theaceae (Tea family), e.g. camellia
Definitions
- This invention relates to a composition, preferably in the form of a beverage, whereby cellular hydration and drinkability are enhanced by the combination of green tea solids with selected levels and types of electrolytes and carbohydrates.
- Sweat which is lost from the body during exercise can produce a state of dehydration or hypohydration.
- Associated with dehydration is an impairment of the body's heat dissipation and performance capacity. It is well known that loss of water, electrolytes, and depletion of carbohydrates are the primary causes of fatigue which can impair work capacity. To maintain performance it is necessary to replace the lost water, electrolytes, carbohydrates and other nutrients.
- WO91/12734 also discloses aqueous beverage compositions containing essential electrolytes and sweeteners, the compositions having an osmolality of from 100 to 270 mOs/l.
- Representative of the prior art is also US 4 946 701, which relates to beverage compositions with flavanols and flavorants. Flavanols are used in these compositions for their relaxing effect.
- the invention described herein is a novel composition which surprisingly provides enhanced cellular hydration while avoiding the premature cessation of drinking. Further, users of the product report lower levels of fatigue, and increased cognitive performance after heat dehydration when the novel composition is used.
- An object of the present invention is to provide beverage compositions which facilitate the distribution of fluid throughout the body, particularly at the cellular level.
- Another object of this invention is to provide thirst quenching beverage compositions.
- Still another object of the present invention is to provide beverage compositions with increased drinkability.
- the subject invention relates to a liquid composition
- a liquid composition comprising:
- a dry composition comprising:
- a method of rapidly rehydrating human or animal cells which have been dehydrated through loss of water and minerals by the ingestion of these compositions is also described.
- This product can be administered as a powder or as a tablet.
- the term “comprising” means various components can be conjointly employed in the beverages of this invention. Accordingly, the terms “consisting essentially of” and “consisting of” are embodied in the term comprising.
- the term “drinkability” means the volume of beverage consumed per drinking occasion. Beverages with enhanced drinkability can be consumed in large volumes without a feeling of fullness or satisfaction.
- the term "thirst quenching” relates to the physiological ability of a beverage to rapidly deliver water through the human digestive system and distribute it throughout the body and into the cells.
- beverage composition means a composition that is single strength and ready to drink.
- beverage concentrate refers to a concentrate that is in liquid form.
- the concentrate is usually formulated to provide a drinkable beverage composition when reconstituted or diluted with water.
- the composition can also be made in an essentially dry mixture form.
- the essentially dry mixture can be in the form of either a powder or a tablet. These compositions are referred to herein as a "dry composition.”
- tea materials refers to teas which include materials obtained from the genus Camellia including Camellia sinensis and Camellia assaimica , for instance, freshly gathered tea leaves, fresh tea leaves that are dried immediately after gathering, fresh tea leaves that have been heat treated before drying to inactivate any enzymes present, unfermented tea, fermented tea, instant green fermented tea, partially fermented tea leaves and aqueous extracts of these leaves.
- Tea materials are tea leaves, their extracts, tea plant stems and other plant materials which are related.
- Members of the genus Phyllanthus , Catechu gambir or Uncaria family of tea plants can also be used. Mixtures of unfermented, partially fermented and fermented, teas can be used.
- tea solids refers to solids extracted from tea materials.
- the tea materials used in the present composition must contain unoxidized, unpolymerized flavanols.
- tea extract refers to an aqueous solution obtained from the extraction of tea materials. This includes the flavanols and caffeine that is present.
- tea extract also encompasses aqueous solutions which have been concentrated or dried.
- flavanols or “catechins” means primarily catechin, epicatechins, and their derivatives. These derivatives include the sugar salts, sugar esters, and other edible physiologically available derivatives. Green tea solids contain these flavanols. Black tea, fruits, and other natural sources also contain these flavanols but to a lesser degree.
- the preferred flavanols are catechin, epicatechin, gallocatechin, epigallocatechin, epicatechin gallate, and epigallocatechin gallate.
- the beverage compositions described herein have been shown to improve cognitive performance after, and decrease the recovery time from, dehydration relative to water in individuals subjected to heat-induced dehydration.
- the invention comprises flavanols, which significantly enhances cellular rehydration.
- the body's physiological response to exercise or environmental exposure is greatly enhanced compared to the response when the body receives no fluids, receives only water, or receives commercial beverages which contain electrolytes and a sugar source in addition to water.
- the cellular hydration advantage of the novel beverage compositions described can be clearly measured using Multi-frequency Bio-Impedance Spectroscopy.
- the beverage compositions of this invention may be consumed by persons engaged in vigorous activity, such as athletes. It may also be consumed by people doing strenuous work, especially in hot environments, or by people who have suffered the loss of body fluids and electrolytes as a result of some illness or disease.
- the beverage composition of this invention may also be consumed by anyone as a supplement to normal dietetic requirements for energy and/or water.
- the beverage compositions of the present invention may be manufactured and sold as a single-strength beverage for direct consumption by the consumer.
- the product may be in the form of a syrup, an aqueous concentrate, a dry powder, or granules which are diluted with water to yield a beverage which fulfills all the requirements of this invention.
- the product may be in the form a tablet which can be taken with water.
- the flavanols are natural substances present in a variety of plants (e.g. fruits, vegetables, flowers).
- the flavanols used in present invention can be extracted from fruit, vegetables, green tea or other natural sources by any suitable method well known to those skilled in the art. For example, extraction with ethyl acetate or chlorinated solvents is one way to isolate flavanols or catechins from green tea; or, they may be prepared by synthetic or other appropriate chemical methods.
- Flavanols, including catechin, epicatechin, and their derivatives are commercially available.
- the flavanols may be extracted from either a single plant or mixtures of plants.
- the preferred flavanols are obtained by the extraction of plants, e.g. green tea and related plants. Many fruits, vegetables, and flowers contain flavanols but to a lesser degree. Plants containing flavanols are known to those skilled in the art. Examples of the most common flavanols which are obtained from extraction of tea plants and other members of the catechu gambir or (Uncaria family) are catechin, epicatechin, gallocatechin, epigallocatechin, epicatechin gallate, epigallocatechin gallate.
- the preferred source of flavanols in the beverage composition of the present invention is green tea. It is believed that the green tea and in particular the flavonols present in green tea when incorporated into the beverage are responsible for the observed enhanced cellular rehydration.
- the flavanols may be in the form of a tea extract.
- the tea extract can be obtained from the extraction of unfermented teas, fermented teas, partially fermented teas and mixtures thereof as long as the unoxidized flavanols come within the specified range.
- the tea extracts are obtained from the extraction of unfermented and partially fermented teas.
- the most preferred tea extracts are obtained from green tea. Both hot and cold extracts can be used in the present invention. Suitable methods for obtaining tea extracts are well known, see, for example, U.S. 4,935,256 to Tsai, issued June 1990; U.S. 4,680,193 to Lunder, issued July 1987; and U.S. 4,668,525 to Creswick, issued May 26, 1987.
- a particularly preferred method for obtaining a tea extract is described, for example in co-pending application Serial Number 08/178/702, filed January 10, 1994.
- the drinkable beverage of the present invention comprises 0.01% to 0.35% unoxidized, unpolymerized flavanols, preferably from 0.02% to 0.2%, equally preferred from 0.025% to 0.1% and most preferably from 0.03% to 0.075% unoxidized, unpolymerized flavanols.
- the drinkable beverage contain from 0.0% to 0.04% caffeine, preferably 0.01% to 0.03%, and most preferably from 0.013% to 0.02% caffeine in addition to the unoxidized, unpolymerized flavanols.
- the total amount of caffeine includes the amount of caffeine naturally present in the tea extract, flavoring agent, and other ingredients as well as any added caffeine.
- the electrolytes and ionic components for the present invention are usually, but not necessarily, obtainable from their corresponding water-soluble and non-toxic salts. They are also present in fruit juices and in the tea extract. Unless otherwise defined, the amount of electrolytes or ionic components in the beverage is based on those present in the final drinkable beverage composition.
- the electrolyte concentration is of the ion only and not the salt. Some of the less soluble salts must be "solubilized" in water, or in water having an acidic pH, in order to be useful in the present invention.
- the potassium ion component can be provided by any salt such as the chloride, carbonate, sulfate, acetate, bicarbonate, citrate, phosphate, hydrogen phosphate, tartrate, sorbate and the like, or mixtures thereof or as a component of added fruit juice or tea.
- the potassium ions are preferably present in the drinkable beverage composition of the present invention in an amount of at least 0.005% to 0.08%, preferably from 0.01% to 0.06% and most preferably from 0.02% to 0.04%.
- the sodium ion component can be obtained from any readily available sodium salt, such as the chloride, carbonate, bicarbonate, citrate, phosphate, hydrogen phosphate, tartrate, benzoate and the like, and mixtures thereof or as a component of added fruit juice or tea. It is important in the present invention that the sodium concentration be low enough to facilitate the absorption of water by osmosis and not osmotically draw water out of the body into the intestine. The concentration of sodium needed to do this is preferably lower than that of plasma sodium.
- the sodium ions are present in the drinkable beverage composition of the present invention in an amount of at least 0.01% to 0.3% preferably in an amount of from 0.02% to 0.2%, and more preferably from 0.04% to 0.15%.
- the composition can additionally contain chloride ion from 0.01% to 0.10%, preferably from 0.03% to 0.1% and most preferably from 0.05% to 0.09%.
- the chloride ion component can be provided by a salt such as sodium chloride or potassium chloride. Other ions such as calcium and magnesium may also be added. These ions may also be provided as a salt.
- the total level of ions present includes the amount naturally present in the beverage along with any added ion addition. For example, if sodium chloride is added, the amount of sodium ion and amount of chloride ion would be included in the total amount of each ion accordingly.
- the beverages of the present invention also contains soluble carbohydrates.
- the carbohydrates can be sweeteners as well as energy sources. In selecting carbohydrates for use in the present beverage it is important that the levels chosen allow a sufficient rate of stomach emptying and intestinal absorption to be effective.
- the carbohydrate can be a mixture of glucose and fructose or be a carbohydrate which hydrolyzes or otherwise forms glucose and fructose in the digestive track.
- the term "carbohydrate” refers to monosaccharides, oligosaccharides, complex polysaccharides, or mixtures thereof.
- the monosaccharides include tetroses, pentoses, hexoses, and ketohexoses.
- hexoses are aldohexoses such as glucose, known as grape sugar.
- the amount of glucose used for the drinkable beverage composition of the present invention preferably is from 0.05% to 10%, more preferably from 1.0% to 5.0% and most preferably from 1.5% to 3%.
- Fructose known as fruit sugar, is a ketohexose.
- the amount of fructose present in the drinkable beverage is from 0.05% to 10%, preferably from 1.0% to 5%, and most preferably from 1.5% to 3%.
- the composition herein must contain these two sugars and/or carbohydrates that form these sugars in the body (i.e. sucrose, maltodextrin, corn syrups, high frutose corn syrups).
- An important class of carbohydrates is a disaccharide.
- An example of a disaccharide is sucrose, know as cane sugar or beet sugar.
- the amount of sucrose present in the drinkable beverage composition of the present invention is from 1% to 20%, more preferably from 2.0% to 10.0%, and most preferably from 3% to 6%.
- the desired total carbohydrate level is from 0.01% to 20%, preferably from 0.5% to 15% and most preferably from 3% to 6%.
- maltodextrin One of the complex carbohydrates usable for the present invention is maltodextrin.
- Maltodextrins are a form of complex carbohydrate molecule several glucose units in length. They are spray-dried carbohydrate ingredients made by controlled hydrolysis of corn starch. The dextrose equivalence ("D.E.") of maltodextrins provide a good index of the degree of starch polymer hydrolysis.
- the amount of maltodextrin used in the drinkable beverage composition is 0% to 10%, preferably from 1% to 4%.
- the preferred maltodextrins are those with a DE up to 20.
- the preferred carbohydrate of the present invention is comprised of a combination of fructose and glucose to achieve an energy source capable of providing needed fuel values as the demand thereof may vary. Since sucrose is hydrolyzed to fructose and glucose in the digestive tract it can be used as a source of fructose and glucose. Each of these sugars is an energy food fully utilizable by cells of the body.
- the total carbohydrates used in the present invention are preferably in the amount of from 0.1% to 20% of the total weight of the drinkable beverage composition.
- the total amount of carbohydrate include any added carbohydrate as well as those naturally present in the fruit juice or tea extract.
- a carbohydrate derivative, polyhydric alcohol, such as glycerol may also be used in the present invention to provide a source of sweetness and to provide energy such that it is readily absorbed and distributed throughout the body.
- glycerol is not essential to achieve the advantages of the present invention.
- amounts of from 0.1% to 15%, preferably from 6% to 10% glycerol can be used in the present invention.
- non-caloric sweeteners can be used in conjunction with at least 0.1% carbohydrate.
- sweeteners include aspartame, saccharine, cyclamates, acesulfam-K, L-aspartyl-L-phenylalanine lower alkyl ester sweeteners, L-aspartyl-D-alanine amides as disclosed in US patent 4,411,925 to Brennan, et al (1983), L-aspartyl-D-serine amides disclosed in US 4,399,163 to Brennan et al (1983), L-aspartyl-hydroxymethyl alkane amide sweeteners disclosed in U.S.
- ingredients include natural and synthetically prepared flavoring agents, natural and synthetically prepared colors, preservatives, acidulants, gums, emulsifiers, oils and vitamins. Flavoring Agents
- a flavoring agent is recommended for the beverage compositions of this invention in order to enhance the palatability.
- Any natural or synthetic flavor agent can be used in the present invention.
- Flavoring agents can be selected from a fruit juice, a fruit flavor, a botanical flavor or mixtures thereof.
- tea flavors preferably green tea or black tea flavors, together with fruit juices has an appealing taste.
- Preferred juices are apple, pear, lemon, lime, mandarin, grapefruit, cranberry, orange, strawberry, grape, kiwi, pineapple, passion fruit, mango, guava, raspberry and cherry.
- Citrus juices, preferably grapefruit, orange, lemon, lime, mandarin and juices of mango, passion fruit and guava, or mixtures thereof are most preferred.
- Preferred natural flavors are jasmine, chamomile, rose hip, peppermint, haw, chrysanthemum, water chestnut, sugar cane, lychee, bamboo shoots and the like.
- the fruit juices can be present as the base to which the flavanols and other ingredients are added or used as the flavoring agent.
- the fruit juice is present in an amount of from 0.5% to 50%, and more preferably from 5.0% to 30%, by weight of the beverage. This concentration is based on the single strength of the beverage.
- Fruit flavors, botanical flavors, tea flavors and mixtures thereof can also be used as the flavoring agent.
- Particularly preferred fruit flavors are the citrus flavors including orange flavors, lemon flavors, lime flavors and grapefruit flavors.
- citrus flavors a variety of other fruit flavors can be used such as apple flavors, grape flavors, raspberry flavors, cranberry flavors, cherry flavors, pineapple flavors and the like.
- These fruit flavors can be derived from natural sources such as fruit juices and flavor oils, or else be synthetically prepared.
- the flavor agent can also comprise a blend of various flavors e.g. lemon and lime flavors, citrus flavors and selected spices (the typical cola soft drink flavor) etc. If desired the flavor in the flavoring agent may be formed into emulsion droplets which are then dispersed in the beverage drink. Because these droplets usually have a specific gravity less than that of water and would therefore form a separate phase, weighting agents (which can also act as clouding agents) can be used to keep the emulsion droplets dispersed in the beverage. Examples of such weighting agents are brominated vegetable oils (BVO) and resin esters, in particular the ester gums. See L.F. Green, Developments in Soft Drinks Technology, Vol. 1 (Applied Science Publishers Ltd. 1978) pp.
- BVO brominated vegetable oils
- resin esters in particular the ester gums. See L.F. Green, Developments in Soft Drinks Technology, Vol. 1 (Applied Science Publishers Ltd. 1978) pp.
- weighting and clouding agents in liquid beverages.
- the flavoring agents are conventionally available as concentrates or extracts or in the form of synthetically produced flavoring esters, alcohols, aldehydes, terpenes, sesquiterpenes, and the like.
- such flavoring agents are added in quantities in the amount of from 0.001% to 2%, preferably from 0.02% to 0.09 %, by weight of the beverage.
- coloring agents can also be added into the drinkable beverage compositions or beverage concentrates of the present invention. Any soluble coloring agents approved for food use can be utilized for the present invention.
- preservatives such as sorbic acid, benzoic acid, hexametaphosphate and salts thereof, can be added into the drinkable beverage composition or beverage concentrate of the present invention.
- the composition can contain an acidulant.
- an acidulant This is intended to describe edible acids such as malic, citric, tartaric, fumaric and the like which are commonly used in beverage drinks.
- An amount of an acidulant may be used to maintain a pH of less than 4.6.
- the beverage has a pH of from 2.5 to 4.0. This will enable the beverage to remain microbially safe.
- Organic as well as inorganic edible acids may be used to adjust the pH of the beverage.
- the acids can be present in their undissociated form or else as their respective salts, for example, potassium or sodium hydrogen phosphate, potassium or sodium dihydrogen phosphate salts.
- the preferred acids are edible organic acids which include citric acid, malic acid, fumaric acid, adipic acid, phosphoric acid, gluconic acid, tartaric acid, ascorbic acid, acetic acid, phosphoric acid or mixtures thereof.
- the most preferred acids are citric and malic acids.
- the acidulant can also serve as an antioxidant to stabilize beverage components.
- antioxidants include but are not limited to ascorbic acid, EDTA (Ethylenediaminetetraacetic acid) and salts thereof.
- Gums, emulsifiers and oils can also be included in the beverage for texture and opacity purposes.
- Typical ingredients include guar gum, xanthan gum, alginates, carboxymethylcellulose (CMC), mono-di glycerides, lecithin, starches, pectin, pulp, cotton seed oil and vegetable oil.
- the beverage compositions can additionally comprise from 0% to 150% of the U. S. RDA of vitamins such that the vitamins are chemically and physically compatible with the essential elements of the beverage composition.
- Vitamins A, C, and E are added.
- Other vitamins such as D and B may also be added.
- Additional minerals can be added to the beverage or dry compositions of the present invention.
- the compositions can comprise from 0% to 150% of the U.S. RDA of minerals such that the minerals are chemically and physically compatible with the function and essential elements of the present invention.
- Preferred minerals are calcium, chromium, copper, fluorine, iodine, iron, magnesium, manganese, phosphorus, selenium, silicon, molybdenum and zinc.
- Particularly preferred minerals are magnesium, phosphorus, and iron.
- the drinkable beverage composition may be prepared by mixing together all of the ingredients. The mixture is dissolved in water and agitated with a mechanical stirrer until all of the ingredients have gone into solution. The preservative, if used, can then be added. The mixture can then be adjusted to a desired pH with an acidulant.
- Single strength fruit juice may also be used to prepare the beverage compositions of the present invention.
- the fruit juice or fruit juice concentrate can be used as the liquid base to which the flavanols and electrolytes are added. Any carbohydrates, water, electrolytes etc. present in the fruit juice or fruit juice concentrates are included in the total amount claimed herein.
- a beverage concentrate syrup can be formed first.
- One way to prepare the concentrate form of the liquid beverage would be to start with less than the required volume of water that is used in the preparation of the drinkable beverage composition.
- Another way would be to partially dehydrate the finally prepared drinkable beverage composition to remove only a portion of the water and any other volatile liquids present. Dehydration can be accomplished in accordance with well known procedure, such as evaporation under vacuum.
- the concentrate can be in the form of a relatively thick, syrupy liquid.
- the syrup is typically formed by adding suitable (i.e. sugar, electrolytes, emulsions) to the beverage concentrate.
- the syrup is then mixed with water to form a finished beverage or finished beverage concentrate.
- the weight ratio of water:syrup is typically from 2:1 (3x syrup) to 5:1 (6x syrup).
- the solid can be in the form of an essentially dry powder or a tablet.
- the dry form can later be reconstituted with a proper amount of water to make the final drinkable beverage composition or taken with the appropriate amount of water to deliver the levels of ingredients stated herein.
- Carbon dioxide can be introduced either into the water to be mixed with the beverage concentrate, or into the drinkable beverage composition, to achieve carbonation.
- the carbonated beverage composition can then be stored in a suitable container and then sealed. See L.F. Green, Developments in Soft Drinks Technology, Vol. 1 (Applied Science Publishers Ltd. 1978), pp. 102-107, for a further description of beverage making, in particular the process for carbonation.
- the essentially dry mixture of the beverage composition can be prepared by blending the proper amounts and ratios of all the required dry ingredients together.
- the finally prepared drinkable beverage composition can be dehydrated to give the essentially dry mixture of the beverage composition.
- the essentially dry mixture either as a powder, granules or tablets, can later be dissolved in a proper amount of water, carbonated or non-carbonated, to make the final drinkable beverage or taken in conjunction with water.
- Essentially dry forms include tablets, capsules, granules and bulk powders. Tablets may contain suitable binders, lubricants, diluents, disintegrating agents, coloring agents, flavoring agents, flow-inducing agents and melting agents. Suitable carriers and excipients that may be used to formulate dry forms of the present invention are described in U.S. Patent 3,903,297, Rober, issued September 2, 1975. Techniques and compositions for making dry forms useful in the methods of this invention are described in the following references; 7 Modern Pharmaceutics, Chapters 9 and 10 (Banker & Rodes, editors, 1979); Liberman et al.; Pharmaceutical Dosage Forms: Tablets (1981); and Ansel, Introduction to Pharmaceutical Dosage Forms, 2nd Edition (1976).
- a typical dry powder comprises from 0.1% to 3.5% flavanols, from 0.1% to 3.0% sodium ions, from 0.05% to 0.8% potassium ions, from 0.5% to 50% fructose, and from 0.5% to 50% glucose. If desired from 1% to 95% sucrose can be used instead of fructose and glucose since sucrose is hydrolyzed to fructose and glucose in the body. The actual concentration of the ingredients in the dry powder will depend upon the amount of dilution or the amount of water consumed.
- a drinkable beverage composition is prepared by combining the following ingredients:
- a beverage composition is prepared by blending the following ingredients: Ingredients Wt. % Fruit Juice 1.7 Juice Concentrate 0.64 Green Tea Extract 63 Lemon Lime Flavoring 0.3 Aspartame 0.25 Ascorbic Acid 0.1 Sodium Chloride 0.035 Colorant 0.1 Sodium Citrate 0.4 Emulsion 1.6 Water 31.875
- the beverages are the beverage prepared according to Example II, water, commercial carbohydrate-electrolyte beverage 1 (CE-1), or commercial carbohydrate-electrolyte beverage 2 (CE-2).
- CE-1 commercial carbohydrate-electrolyte beverage 1
- CE-2 commercial carbohydrate-electrolyte beverage 2
- the order of beverage consumption is randomized separately for each subject.
- the subject is allowed to drink as much of each beverage as they wish for 30 minutes after exercise. All beverages are lime flavor except water.
- the beverage according to Example II is consumed in a greater volume than water and both of the CE beverages.
Landscapes
- Health & Medical Sciences (AREA)
- Life Sciences & Earth Sciences (AREA)
- Natural Medicines & Medicinal Plants (AREA)
- Chemical & Material Sciences (AREA)
- Engineering & Computer Science (AREA)
- Food Science & Technology (AREA)
- Polymers & Plastics (AREA)
- Nutrition Science (AREA)
- Mycology (AREA)
- Medical Informatics (AREA)
- Animal Behavior & Ethology (AREA)
- Botany (AREA)
- Alternative & Traditional Medicine (AREA)
- Medicinal Chemistry (AREA)
- Microbiology (AREA)
- Veterinary Medicine (AREA)
- Pharmacology & Pharmacy (AREA)
- Epidemiology (AREA)
- Biotechnology (AREA)
- General Health & Medical Sciences (AREA)
- Public Health (AREA)
- Dispersion Chemistry (AREA)
- Inorganic Chemistry (AREA)
- Tea And Coffee (AREA)
- Non-Alcoholic Beverages (AREA)
- Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
- Acyclic And Carbocyclic Compounds In Medicinal Compositions (AREA)
Abstract
Description
- This invention relates to a composition, preferably in the form of a beverage, whereby cellular hydration and drinkability are enhanced by the combination of green tea solids with selected levels and types of electrolytes and carbohydrates.
- Moderate physical activity, prolonged exercise or working in hot, humid environments causes excessive loss of minerals and body fluids through perspiration and breathing. Physical activity, such as exercise, particularly in the heat, places a great metabolic demand on a human body. Heat generated during exercise is dissipated during sweating.
- Sweat which is lost from the body during exercise can produce a state of dehydration or hypohydration. Associated with dehydration is an impairment of the body's heat dissipation and performance capacity. It is well known that loss of water, electrolytes, and depletion of carbohydrates are the primary causes of fatigue which can impair work capacity. To maintain performance it is necessary to replace the lost water, electrolytes, carbohydrates and other nutrients.
- Attempts have been made to counteract these adverse effects of strenuous activity. Consumption of water helps maintain body temperature and blood volume, but water is absorbed relatively slowly. Products have been developed recently which combine sugar, water, essential electrolytes and other ingredients lost from the body through physical activity. Several well known products are Gatorade Thirst Quencher® , All Sport® and PowerAde® . Other compositions are well known and are described, for example in U.S. 4,874,606 issued to Boyle et al. October 17, 1989 and U.S. 4,322,407 issued to Ko, March 30, 1982.
- WO91/12734 also discloses aqueous beverage compositions containing essential electrolytes and sweeteners, the compositions having an osmolality of from 100 to 270 mOs/l. Representative of the prior art is also US 4 946 701, which relates to beverage compositions with flavanols and flavorants. Flavanols are used in these compositions for their relaxing effect.
- The focus of rehydration (Sports) beverages, has been to replenish lost electrolytes, carbohydrates, and other essential constituents which are lost through dehydration. Only a few address the unmet need of providing rapid cellular hydration and water distribution within the body. Beverage formulas that address cellular needs are described, for example, in U.S. 5,147,650 to Fregly issued September 15, 1992 and U.S. 5,114,723 issued to Stray-Gundersen May 19, 1992.
- Although there are formulas that help to combat some of the unmet needs, many of the commercial beverages cause a feeling of fullness or satisfaction and therefore drinking is stopped before the amount of liquid needed for rehydration is consumed.
- The invention described herein is a novel composition which surprisingly provides enhanced cellular hydration while avoiding the premature cessation of drinking. Further, users of the product report lower levels of fatigue, and increased cognitive performance after heat dehydration when the novel composition is used.
- An object of the present invention is to provide beverage compositions which facilitate the distribution of fluid throughout the body, particularly at the cellular level.
- Another object of this invention is to provide thirst quenching beverage compositions.
- Still another object of the present invention is to provide beverage compositions with increased drinkability.
- These and other objects will become apparent from the following detailed description.
- All percentages herein are by weight unless otherwise specified.
- The subject invention relates to a liquid composition comprising:
- (a) from 0.01% to 0.35% unoxidized, unpolymerized flavanols;
- (b) from 0.01% to 0.3% sodium ions;
- (c) from 0.005% to 0.08% potassium ions;
- (d) from 0.1% to 20% of a carbohydrate which provides
- (i) from 0.05% to 10.0% fructose;
- (ii) from 0.05% to 10.0% glucose; and
- (e) water.
-
- A dry composition comprising:
- (a) from 0.1% to 3.5% unoxidized, unpolymerized flavanols;
- (b) from 0.1% to 3.0% sodium ions;
- (c) from 0.05% to 0.8% potassium ions;
- (d) from 1.0% to 95% of a carbohydrate which provides
- (i) from 0.5% to 50% fructose;
- (ii) from 0.5% to 50% glucose.
-
- A method of rapidly rehydrating human or animal cells which have been dehydrated through loss of water and minerals by the ingestion of these compositions is also described. This product can be administered as a powder or as a tablet.
- As used herein, the term "comprising" means various components can be conjointly employed in the beverages of this invention. Accordingly, the terms "consisting essentially of" and "consisting of" are embodied in the term comprising.
- As used herein, the term "drinkability" means the volume of beverage consumed per drinking occasion. Beverages with enhanced drinkability can be consumed in large volumes without a feeling of fullness or satisfaction.
- As used herein, the term "thirst quenching" relates to the physiological ability of a beverage to rapidly deliver water through the human digestive system and distribute it throughout the body and into the cells.
- As used herein, the term "beverage composition" means a composition that is single strength and ready to drink.
- As used herein, "beverage concentrate" refers to a concentrate that is in liquid form. The concentrate is usually formulated to provide a drinkable beverage composition when reconstituted or diluted with water. The composition can also be made in an essentially dry mixture form. The essentially dry mixture can be in the form of either a powder or a tablet. These compositions are referred to herein as a "dry composition."
- As used herein, the term "tea materials" refers to teas which include materials obtained from the genus Camellia including Camellia sinensis and Camellia assaimica, for instance, freshly gathered tea leaves, fresh tea leaves that are dried immediately after gathering, fresh tea leaves that have been heat treated before drying to inactivate any enzymes present, unfermented tea, fermented tea, instant green fermented tea, partially fermented tea leaves and aqueous extracts of these leaves. Tea materials are tea leaves, their extracts, tea plant stems and other plant materials which are related. Members of the genus Phyllanthus, Catechu gambir or Uncaria family of tea plants can also be used. Mixtures of unfermented, partially fermented and fermented, teas can be used.
- As used herein, the term "tea solids" refers to solids extracted from tea materials. The tea materials used in the present composition must contain unoxidized, unpolymerized flavanols.
- As used herein, the term "tea extract" refers to an aqueous solution obtained from the extraction of tea materials. This includes the flavanols and caffeine that is present. The term "tea extract" also encompasses aqueous solutions which have been concentrated or dried.
- As used herein "flavanols" or "catechins" means primarily catechin, epicatechins, and their derivatives. These derivatives include the sugar salts, sugar esters, and other edible physiologically available derivatives. Green tea solids contain these flavanols. Black tea, fruits, and other natural sources also contain these flavanols but to a lesser degree. The preferred flavanols are catechin, epicatechin, gallocatechin, epigallocatechin, epicatechin gallate, and epigallocatechin gallate.
- All percentages herein are by weight unless otherwise specified.
- The beverage compositions described herein have been shown to improve cognitive performance after, and decrease the recovery time from, dehydration relative to water in individuals subjected to heat-induced dehydration. Specifically, the invention comprises flavanols, which significantly enhances cellular rehydration.
- When the beverage compositions of the present invention are administered, the body's physiological response to exercise or environmental exposure is greatly enhanced compared to the response when the body receives no fluids, receives only water, or receives commercial beverages which contain electrolytes and a sugar source in addition to water. The cellular hydration advantage of the novel beverage compositions described can be clearly measured using Multi-frequency Bio-Impedance Spectroscopy.
- The replacement of body fluids and electrolytes lost by those individuals engaged in moderate to strenuous activities is essential if smooth and efficient muscle function is to be maintained. Water and electrolytes are lost as the body regulates its temperature through perspiration. Those individuals undergoing work, exercise, or any activity requiring moderate to strenuous use of the muscles and/or the loss of body water and electrolytes need rapid replacement of the lost body fluids and electrolytes.
- The beverage compositions of this invention may be consumed by persons engaged in vigorous activity, such as athletes. It may also be consumed by people doing strenuous work, especially in hot environments, or by people who have suffered the loss of body fluids and electrolytes as a result of some illness or disease. The beverage composition of this invention may also be consumed by anyone as a supplement to normal dietetic requirements for energy and/or water.
- The beverage compositions of the present invention may be manufactured and sold as a single-strength beverage for direct consumption by the consumer. The product may be in the form of a syrup, an aqueous concentrate, a dry powder, or granules which are diluted with water to yield a beverage which fulfills all the requirements of this invention. Alternatively, the product may be in the form a tablet which can be taken with water.
- An important ingredient in the beverage composition of the present invention are the flavanols. The flavanols are natural substances present in a variety of plants (e.g. fruits, vegetables, flowers). The flavanols used in present invention can be extracted from fruit, vegetables, green tea or other natural sources by any suitable method well known to those skilled in the art. For example, extraction with ethyl acetate or chlorinated solvents is one way to isolate flavanols or catechins from green tea; or, they may be prepared by synthetic or other appropriate chemical methods. Flavanols, including catechin, epicatechin, and their derivatives are commercially available.
- The flavanols may be extracted from either a single plant or mixtures of plants. The preferred flavanols are obtained by the extraction of plants, e.g. green tea and related plants. Many fruits, vegetables, and flowers contain flavanols but to a lesser degree. Plants containing flavanols are known to those skilled in the art. Examples of the most common flavanols which are obtained from extraction of tea plants and other members of the catechu gambir or (Uncaria family) are catechin, epicatechin, gallocatechin, epigallocatechin, epicatechin gallate, epigallocatechin gallate.
- The preferred source of flavanols in the beverage composition of the present invention is green tea. It is believed that the green tea and in particular the flavonols present in green tea when incorporated into the beverage are responsible for the observed enhanced cellular rehydration.
- The flavanols may be in the form of a tea extract. The tea extract can be obtained from the extraction of unfermented teas, fermented teas, partially fermented teas and mixtures thereof as long as the unoxidized flavanols come within the specified range. Preferably the tea extracts are obtained from the extraction of unfermented and partially fermented teas. The most preferred tea extracts are obtained from green tea. Both hot and cold extracts can be used in the present invention. Suitable methods for obtaining tea extracts are well known, see, for example, U.S. 4,935,256 to Tsai, issued June 1990; U.S. 4,680,193 to Lunder, issued July 1987; and U.S. 4,668,525 to Creswick, issued May 26, 1987. A particularly preferred method for obtaining a tea extract is described, for example in co-pending application Serial Number 08/178/702, filed January 10, 1994.
- The drinkable beverage of the present invention comprises 0.01% to 0.35% unoxidized, unpolymerized flavanols, preferably from 0.02% to 0.2%, equally preferred from 0.025% to 0.1% and most preferably from 0.03% to 0.075% unoxidized, unpolymerized flavanols.
- It is preferred that the drinkable beverage contain from 0.0% to 0.04% caffeine, preferably 0.01% to 0.03%, and most preferably from 0.013% to 0.02% caffeine in addition to the unoxidized, unpolymerized flavanols. The total amount of caffeine includes the amount of caffeine naturally present in the tea extract, flavoring agent, and other ingredients as well as any added caffeine.
- Among the major physiological electrolytes are potassium and sodium. The electrolytes and ionic components for the present invention are usually, but not necessarily, obtainable from their corresponding water-soluble and non-toxic salts. They are also present in fruit juices and in the tea extract. Unless otherwise defined, the amount of electrolytes or ionic components in the beverage is based on those present in the final drinkable beverage composition. The electrolyte concentration is of the ion only and not the salt. Some of the less soluble salts must be "solubilized" in water, or in water having an acidic pH, in order to be useful in the present invention.
- The potassium ion component can be provided by any salt such as the chloride, carbonate, sulfate, acetate, bicarbonate, citrate, phosphate, hydrogen phosphate, tartrate, sorbate and the like, or mixtures thereof or as a component of added fruit juice or tea. The potassium ions are preferably present in the drinkable beverage composition of the present invention in an amount of at least 0.005% to 0.08%, preferably from 0.01% to 0.06% and most preferably from 0.02% to 0.04%.
- Likewise, the sodium ion component can be obtained from any readily available sodium salt, such as the chloride, carbonate, bicarbonate, citrate, phosphate, hydrogen phosphate, tartrate, benzoate and the like, and mixtures thereof or as a component of added fruit juice or tea. It is important in the present invention that the sodium concentration be low enough to facilitate the absorption of water by osmosis and not osmotically draw water out of the body into the intestine. The concentration of sodium needed to do this is preferably lower than that of plasma sodium. The sodium ions are present in the drinkable beverage composition of the present invention in an amount of at least 0.01% to 0.3% preferably in an amount of from 0.02% to 0.2%, and more preferably from 0.04% to 0.15%.
- In addition to potassium and sodium ions, the composition can additionally contain chloride ion from 0.01% to 0.10%, preferably from 0.03% to 0.1% and most preferably from 0.05% to 0.09%. The chloride ion component can be provided by a salt such as sodium chloride or potassium chloride. Other ions such as calcium and magnesium may also be added. These ions may also be provided as a salt. The total level of ions present includes the amount naturally present in the beverage along with any added ion addition. For example, if sodium chloride is added, the amount of sodium ion and amount of chloride ion would be included in the total amount of each ion accordingly.
- The beverages of the present invention also contains soluble carbohydrates. The carbohydrates can be sweeteners as well as energy sources. In selecting carbohydrates for use in the present beverage it is important that the levels chosen allow a sufficient rate of stomach emptying and intestinal absorption to be effective. The carbohydrate can be a mixture of glucose and fructose or be a carbohydrate which hydrolyzes or otherwise forms glucose and fructose in the digestive track.
- As used herein, the term "carbohydrate" refers to monosaccharides, oligosaccharides, complex polysaccharides, or mixtures thereof. The monosaccharides include tetroses, pentoses, hexoses, and ketohexoses. Examples of hexoses are aldohexoses such as glucose, known as grape sugar. The amount of glucose used for the drinkable beverage composition of the present invention preferably is from 0.05% to 10%, more preferably from 1.0% to 5.0% and most preferably from 1.5% to 3%. Fructose, known as fruit sugar, is a ketohexose. Preferably, the amount of fructose present in the drinkable beverage is from 0.05% to 10%, preferably from 1.0% to 5%, and most preferably from 1.5% to 3%. The composition herein must contain these two sugars and/or carbohydrates that form these sugars in the body (i.e. sucrose, maltodextrin, corn syrups, high frutose corn syrups). An important class of carbohydrates is a disaccharide. An example of a disaccharide is sucrose, know as cane sugar or beet sugar. Preferably, the amount of sucrose present in the drinkable beverage composition of the present invention is from 1% to 20%, more preferably from 2.0% to 10.0%, and most preferably from 3% to 6%.
- The desired total carbohydrate level is from 0.01% to 20%, preferably from 0.5% to 15% and most preferably from 3% to 6%.
- One of the complex carbohydrates usable for the present invention is maltodextrin. Maltodextrins are a form of complex carbohydrate molecule several glucose units in length. They are spray-dried carbohydrate ingredients made by controlled hydrolysis of corn starch. The dextrose equivalence ("D.E.") of maltodextrins provide a good index of the degree of starch polymer hydrolysis. The amount of maltodextrin used in the drinkable beverage composition is 0% to 10%, preferably from 1% to 4%. The preferred maltodextrins are those with a DE up to 20.
- The preferred carbohydrate of the present invention is comprised of a combination of fructose and glucose to achieve an energy source capable of providing needed fuel values as the demand thereof may vary. Since sucrose is hydrolyzed to fructose and glucose in the digestive tract it can be used as a source of fructose and glucose. Each of these sugars is an energy food fully utilizable by cells of the body.
- The total carbohydrates used in the present invention are preferably in the amount of from 0.1% to 20% of the total weight of the drinkable beverage composition. The total amount of carbohydrate include any added carbohydrate as well as those naturally present in the fruit juice or tea extract.
- A carbohydrate derivative, polyhydric alcohol, such as glycerol may also be used in the present invention to provide a source of sweetness and to provide energy such that it is readily absorbed and distributed throughout the body. However, the presence of glycerol is not essential to achieve the advantages of the present invention. When desired, amounts of from 0.1% to 15%, preferably from 6% to 10% glycerol can be used in the present invention.
- For diet beverages, non-caloric sweeteners can be used in conjunction with at least 0.1% carbohydrate. Examples of such sweeteners include aspartame, saccharine, cyclamates, acesulfam-K, L-aspartyl-L-phenylalanine lower alkyl ester sweeteners, L-aspartyl-D-alanine amides as disclosed in US patent 4,411,925 to Brennan, et al (1983), L-aspartyl-D-serine amides disclosed in US 4,399,163 to Brennan et al (1983), L-aspartyl-hydroxymethyl alkane amide sweeteners disclosed in U.S. 4,338,346 issued to Brand (1982), L-aspartyl-1-hydroxyethylalkane amide sweeteners disclosed in US 4,423,029 to Rizzi (1983), glycyrrhizins, synthetic alkoxy aromatics, etc. Lo Han Guo juice, stevioside and other natural sources of sweeteners can also be used.
- Other minor ingredients can be included in the beverages of the present invention. Such ingredients include natural and synthetically prepared flavoring agents, natural and synthetically prepared colors, preservatives, acidulants, gums, emulsifiers, oils and vitamins. Flavoring Agents
- A flavoring agent is recommended for the beverage compositions of this invention in order to enhance the palatability. Any natural or synthetic flavor agent can be used in the present invention. Flavoring agents can be selected from a fruit juice, a fruit flavor, a botanical flavor or mixtures thereof. In particular the combination of tea flavors, preferably green tea or black tea flavors, together with fruit juices has an appealing taste. Preferred juices are apple, pear, lemon, lime, mandarin, grapefruit, cranberry, orange, strawberry, grape, kiwi, pineapple, passion fruit, mango, guava, raspberry and cherry. Citrus juices, preferably grapefruit, orange, lemon, lime, mandarin and juices of mango, passion fruit and guava, or mixtures thereof are most preferred. Preferred natural flavors are jasmine, chamomile, rose hip, peppermint, haw, chrysanthemum, water chestnut, sugar cane, lychee, bamboo shoots and the like.
- The fruit juices can be present as the base to which the flavanols and other ingredients are added or used as the flavoring agent. When used as the flavoring agent, the fruit juice is present in an amount of from 0.5% to 50%, and more preferably from 5.0% to 30%, by weight of the beverage. This concentration is based on the single strength of the beverage.
- Fruit flavors, botanical flavors, tea flavors and mixtures thereof can also be used as the flavoring agent. Particularly preferred fruit flavors are the citrus flavors including orange flavors, lemon flavors, lime flavors and grapefruit flavors. Besides citrus flavors, a variety of other fruit flavors can be used such as apple flavors, grape flavors, raspberry flavors, cranberry flavors, cherry flavors, pineapple flavors and the like. These fruit flavors can be derived from natural sources such as fruit juices and flavor oils, or else be synthetically prepared.
- The flavor agent can also comprise a blend of various flavors e.g. lemon and lime flavors, citrus flavors and selected spices (the typical cola soft drink flavor) etc. If desired the flavor in the flavoring agent may be formed into emulsion droplets which are then dispersed in the beverage drink. Because these droplets usually have a specific gravity less than that of water and would therefore form a separate phase, weighting agents (which can also act as clouding agents) can be used to keep the emulsion droplets dispersed in the beverage. Examples of such weighting agents are brominated vegetable oils (BVO) and resin esters, in particular the ester gums. See L.F. Green, Developments in Soft Drinks Technology, Vol. 1 (Applied Science Publishers Ltd. 1978) pp. 87-93 for a further description of the use of weighting and clouding agents in liquid beverages. Typically the flavoring agents are conventionally available as concentrates or extracts or in the form of synthetically produced flavoring esters, alcohols, aldehydes, terpenes, sesquiterpenes, and the like. Typically, such flavoring agents are added in quantities in the amount of from 0.001% to 2%, preferably from 0.02% to 0.09 %, by weight of the beverage.
- If desired, coloring agents can also be added into the drinkable beverage compositions or beverage concentrates of the present invention. Any soluble coloring agents approved for food use can be utilized for the present invention.
- When desired, preservatives, such as sorbic acid, benzoic acid, hexametaphosphate and salts thereof, can be added into the drinkable beverage composition or beverage concentrate of the present invention.
- Also, if desired, the composition can contain an acidulant. This is intended to describe edible acids such as malic, citric, tartaric, fumaric and the like which are commonly used in beverage drinks. An amount of an acidulant may be used to maintain a pH of less than 4.6. Preferably the beverage has a pH of from 2.5 to 4.0. This will enable the beverage to remain microbially safe.
- Organic as well as inorganic edible acids may be used to adjust the pH of the beverage. The acids can be present in their undissociated form or else as their respective salts, for example, potassium or sodium hydrogen phosphate, potassium or sodium dihydrogen phosphate salts. The preferred acids are edible organic acids which include citric acid, malic acid, fumaric acid, adipic acid, phosphoric acid, gluconic acid, tartaric acid, ascorbic acid, acetic acid, phosphoric acid or mixtures thereof. The most preferred acids are citric and malic acids.
- The acidulant can also serve as an antioxidant to stabilize beverage components. Examples of commonly used antioxidant include but are not limited to ascorbic acid, EDTA (Ethylenediaminetetraacetic acid) and salts thereof.
- Gums, emulsifiers and oils can also be included in the beverage for texture and opacity purposes. Typical ingredients include guar gum, xanthan gum, alginates, carboxymethylcellulose (CMC), mono-di glycerides, lecithin, starches, pectin, pulp, cotton seed oil and vegetable oil.
- The beverage compositions can additionally comprise from 0% to 150% of the U. S. RDA of vitamins such that the vitamins are chemically and physically compatible with the essential elements of the beverage composition. Preferably Vitamins A, C, and E are added. Other vitamins such as D and B may also be added.
- Additional minerals can be added to the beverage or dry compositions of the present invention. The compositions can comprise from 0% to 150% of the U.S. RDA of minerals such that the minerals are chemically and physically compatible with the function and essential elements of the present invention. Preferred minerals are calcium, chromium, copper, fluorine, iodine, iron, magnesium, manganese, phosphorus, selenium, silicon, molybdenum and zinc. Particularly preferred minerals are magnesium, phosphorus, and iron.
- The drinkable beverage composition may be prepared by mixing together all of the ingredients. The mixture is dissolved in water and agitated with a mechanical stirrer until all of the ingredients have gone into solution. The preservative, if used, can then be added. The mixture can then be adjusted to a desired pH with an acidulant.
- Single strength fruit juice may also be used to prepare the beverage compositions of the present invention. The fruit juice or fruit juice concentrate can be used as the liquid base to which the flavanols and electrolytes are added. Any carbohydrates, water, electrolytes etc. present in the fruit juice or fruit juice concentrates are included in the total amount claimed herein.
- In making a single strength beverage, a beverage concentrate syrup can be formed first. One way to prepare the concentrate form of the liquid beverage would be to start with less than the required volume of water that is used in the preparation of the drinkable beverage composition. Another way would be to partially dehydrate the finally prepared drinkable beverage composition to remove only a portion of the water and any other volatile liquids present. Dehydration can be accomplished in accordance with well known procedure, such as evaporation under vacuum. The concentrate can be in the form of a relatively thick, syrupy liquid. The syrup is typically formed by adding suitable (i.e. sugar, electrolytes, emulsions) to the beverage concentrate. The syrup is then mixed with water to form a finished beverage or finished beverage concentrate. The weight ratio of water:syrup is typically from 2:1 (3x syrup) to 5:1 (6x syrup).
- The solid can be in the form of an essentially dry powder or a tablet. The dry form can later be reconstituted with a proper amount of water to make the final drinkable beverage composition or taken with the appropriate amount of water to deliver the levels of ingredients stated herein.
- Carbon dioxide can be introduced either into the water to be mixed with the beverage concentrate, or into the drinkable beverage composition, to achieve carbonation. The carbonated beverage composition can then be stored in a suitable container and then sealed. See L.F. Green, Developments in Soft Drinks Technology, Vol. 1 (Applied Science Publishers Ltd. 1978), pp. 102-107, for a further description of beverage making, in particular the process for carbonation.
- The essentially dry mixture of the beverage composition can be prepared by blending the proper amounts and ratios of all the required dry ingredients together. Alternatively, the finally prepared drinkable beverage composition can be dehydrated to give the essentially dry mixture of the beverage composition. The essentially dry mixture, either as a powder, granules or tablets, can later be dissolved in a proper amount of water, carbonated or non-carbonated, to make the final drinkable beverage or taken in conjunction with water.
- Essentially dry forms include tablets, capsules, granules and bulk powders. Tablets may contain suitable binders, lubricants, diluents, disintegrating agents, coloring agents, flavoring agents, flow-inducing agents and melting agents. Suitable carriers and excipients that may be used to formulate dry forms of the present invention are described in U.S. Patent 3,903,297, Rober, issued September 2, 1975. Techniques and compositions for making dry forms useful in the methods of this invention are described in the following references; 7 Modern Pharmaceutics, Chapters 9 and 10 (Banker & Rodes, editors, 1979); Liberman et al.; Pharmaceutical Dosage Forms: Tablets (1981); and Ansel, Introduction to Pharmaceutical Dosage Forms, 2nd Edition (1976).
- A typical dry powder comprises from 0.1% to 3.5% flavanols, from 0.1% to 3.0% sodium ions, from 0.05% to 0.8% potassium ions, from 0.5% to 50% fructose, and from 0.5% to 50% glucose. If desired from 1% to 95% sucrose can be used instead of fructose and glucose since sucrose is hydrolyzed to fructose and glucose in the body. The actual concentration of the ingredients in the dry powder will depend upon the amount of dilution or the amount of water consumed.
- The following examples are given to illustrate the invention.
- A drinkable beverage composition is prepared by combining the following ingredients:
-
Ingredients Wt. % Fruit Juice Concentrate 4.0 Green Tea Solids 0.35 Flavoring 0.06 Sodium Citrate 0.32 Ascorbic Acid 0.01 Aspartame 0.01 Glucose 0.8 Water 94.45 - A beverage composition is prepared by blending the following ingredients:
Ingredients Wt. % Fruit Juice 1.7 Juice Concentrate 0.64 Green Tea Extract 63 Lemon Lime Flavoring 0.3 Aspartame 0.25 Ascorbic Acid 0.1 Sodium Chloride 0.035 Colorant 0.1 Sodium Citrate 0.4 Emulsion 1.6 Water 31.875 - A healthy person who is exposed to temperatures of about 40,5°C (105°F) at 75% humidity for about one hour can consume 835 cc's of a beverage prepared according to Example 1. The expansion of the intra-cellular compartment can be measured using Multi-frequency Bio-Impedance Spectroscopy with a Xitron 4000b spectrometer (Xitron Technologies, Inc.). Measurements of this kind show that the composition of the invention is able to significantly expand the intra-cellular water compartment when compared to commercial beverages containing carbohydrates and electrolytes. The expansion may typically become noticeable when the actual volume consumed is about equal to the amount the person would lose through perspiration during heat exposure. The difference is statistically significant (p=0.051).
EXPANSION OF THE INTRA-CELLULAR WATER COMPARTMENT Beverage prepared according to Example 1 Commercial beverage containing electrolytes and carbohydrates N=8 N=9 646 ± 212 cc 28 ± 200 cc N is number of subjects. - Five human volunteer subjects, each of whom exercises regularly by running a constant distance per day (5 - 8 k), are provided one of four separate beverages at the completion of their usual daily run for four days in a row. The beverages are the beverage prepared according to Example II, water, commercial carbohydrate-electrolyte beverage 1 (CE-1), or commercial carbohydrate-electrolyte beverage 2 (CE-2). The order of beverage consumption is randomized separately for each subject. The subject is allowed to drink as much of each beverage as they wish for 30 minutes after exercise. All beverages are lime flavor except water. The beverage according to Example II is consumed in a greater volume than water and both of the CE beverages.
AVERAGE BEVERAGE VOLUME CONSUMPTION (CC's) AFTER EXERCISE EXAMPLE II BEVERAGE CE-1 CE-2 WATER 1269 cc 1099 cc 977 cc 894cc 100% 87% 77% 70%
Claims (10)
- A fluid composition characterized in that it comprises:(a) from 0.01% to 0.35% unoxidized, unpolymerized flavanols;(b) from 0.01% to 0.3% sodium ions;(c) from 0.005% to 0.08% potassium ions;(d) from 0.1% to 20% of a carbohydrate which provides(i) from 0.05% to 10.0% fructose;(ii) from 0.05% to 10.0% glucose; and(e) water.
- The composition of Claim 1 in which said sodium ions are from 0.02% to 0.2%, said potassium ions are from 0.01% to 0.06%, said carbohydrate is from 2% to 10% and which provides from 1% to 5% fructose and from 1% to 5% glucose.
- The composition of any of Claims 1 or 2 which further comprises from 0.01% to 0.04% caffeine, preferably from 0.013% to 0.03% caffeine.
- The composition of Claim 1, 2 or 3 in which said flavonol concentration is from 0.02% to 0.095%.
- The composition of any of Claims 1, 2, 3 or 4 which further comprise from 0.05% to 0.09% chloride ion.
- A concentrate in the form of a syrup comprising:(a) from 0.03% to 2.1% unoxidized, unpolymerized flavanols;(b) from 0.03% to 1.8% sodium ions;(c) from 0.015% to 0.48% potassium ions;(d) from 0.3% to 70% of a carbohydrate which provides(i) from 0.15% to 50.0% fructose;(ii) from 0.15% to 50.0% glucose; and(e) from 30% to 70% water.
- A dry composition characterized in that it comprises:(a) from 0.1% to 3.5% unoxidized, unpolymerized flavanols;(b) from 0.1% to 3% sodium ions;(c) from 0.05% to 0.8% potassium ions;(d) from 1.0% to 95% of a carbohydrate which provides(i) from 0.5% to 50% fructose; and(ii) from 0.5% to 50% glucose.
- The composition of Claim 7 in which said composition is in the form of a tablet.
- The composition of Claims 6, 7 or 8 further comprising from 0.01% to 0.04% caffeine and 0.03% to 0.1% chloride ion.
- The composition of Claims 6, 7 or 8 further comprising from 0.013% to 0.02% caffeine and 0.03% to 0.1% chloride ion.
Applications Claiming Priority (3)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
US08/253,646 US5464619A (en) | 1994-06-03 | 1994-06-03 | Beverage compositions containing green tea solids, electrolytes and carbohydrates to provide improved cellular hydration and drinkability |
US253646 | 1994-06-03 | ||
PCT/US1995/006508 WO1995033385A1 (en) | 1994-06-03 | 1995-05-23 | Beverage compositions containing green tea solids, electrolytes and carbohydrates to provide improved cellular hydration and drinkability |
Publications (2)
Publication Number | Publication Date |
---|---|
EP0762836A1 EP0762836A1 (en) | 1997-03-19 |
EP0762836B1 true EP0762836B1 (en) | 2001-07-11 |
Family
ID=22961133
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
EP95919908A Expired - Lifetime EP0762836B1 (en) | 1994-06-03 | 1995-05-23 | Beverage compositions containing green tea solids, electrolytes and carbohydrates to provide improved cellular hydration and drinkability |
Country Status (16)
Country | Link |
---|---|
US (2) | US5464619A (en) |
EP (1) | EP0762836B1 (en) |
JP (1) | JP3620600B2 (en) |
CN (1) | CN1075715C (en) |
AT (1) | ATE202900T1 (en) |
AU (1) | AU2555695A (en) |
BR (1) | BR9507835A (en) |
CA (1) | CA2191712C (en) |
DE (1) | DE69521701T2 (en) |
ES (1) | ES2158113T3 (en) |
FI (1) | FI964836A0 (en) |
GR (1) | GR3036880T3 (en) |
HU (1) | HU9603321D0 (en) |
NO (1) | NO965130D0 (en) |
PL (1) | PL317431A1 (en) |
WO (1) | WO1995033385A1 (en) |
Cited By (3)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
WO2008012147A1 (en) | 2006-07-24 | 2008-01-31 | Unilever Plc | Improved beverage |
US8017168B2 (en) | 2006-11-02 | 2011-09-13 | The Coca-Cola Company | High-potency sweetener composition with rubisco protein, rubiscolin, rubiscolin derivatives, ace inhibitory peptides, and combinations thereof, and compositions sweetened therewith |
US9101160B2 (en) | 2005-11-23 | 2015-08-11 | The Coca-Cola Company | Condiments with high-potency sweetener |
Families Citing this family (109)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US5683678A (en) * | 1995-03-09 | 1997-11-04 | The Procter & Gamble Company | Oral compositions |
US6063428A (en) * | 1996-02-26 | 2000-05-16 | The Procter & Gamble Company | Green tea extract subjected to cation exchange treatment and nanofiltration to improve clarity and color |
IL129034A (en) * | 1996-09-20 | 2002-03-10 | Howard Foundation | Flavonol and anthocyanin containing food supplements |
US6238673B1 (en) | 1996-09-20 | 2001-05-29 | The Howard Foundation | Method of producing high flavonol content polyphenol compositions |
US6569446B1 (en) | 1996-09-20 | 2003-05-27 | The Howard Foundation | Solubilization of flavonols |
ATE304798T1 (en) * | 1996-11-12 | 2005-10-15 | Garcia Paul Booth | FORMULA FOR CONTROLLED DELIVERY FOR ENERGY DRINKS |
ES2117595B1 (en) * | 1997-01-28 | 1999-04-01 | Richard Zinos | WATER WITH CAFFEINE |
US6132787A (en) * | 1997-04-25 | 2000-10-17 | The Procter & Gamble Company | Antimicrobial combinations of a sorbate preservative natamycin and a dialkyl dicarbonate useful in treating beverages and other food products and process of making |
US6171635B1 (en) | 1997-05-06 | 2001-01-09 | Iris G Zhao | Coffee substitute |
US20030017998A1 (en) * | 1997-05-16 | 2003-01-23 | Snow Alan D. | Proanthocyanidins for the treatment of amyloid and alpha-synuclein diseases |
MY117538A (en) * | 1997-05-28 | 2004-07-31 | Isegen South Africa Proprietary Ltd | Production of a food acid mixture containing fumaric acid |
EP0919138A1 (en) * | 1997-12-01 | 1999-06-02 | The Procter & Gamble Company | Beverage comprising an effective amount of flavanols as sweetness cutting composition |
EP0919139A1 (en) * | 1997-12-01 | 1999-06-02 | The Procter & Gamble Company | Beverage comprising an effective amount of a sweetness cutting composition |
US6682766B2 (en) | 1997-12-01 | 2004-01-27 | The Procter & Gamble Company | Beverage comprising an effective amount of flavanols as sweetness cutting composition |
DE19820680C1 (en) * | 1998-05-08 | 1999-09-16 | Eckes Granini Gmbh Co Kg | Antioxidant herbal beverage having cardioprotective and collagen-stabilizing effects and lowering blood homocysteine levels |
DE19821920A1 (en) * | 1998-05-15 | 1999-11-18 | Sawo Ag Glarus | Tea concentrate used for making iced or hot tea |
US6544616B2 (en) | 2000-07-21 | 2003-04-08 | Target Technology Company, Llc | Metal alloys for the reflective or the semi-reflective layer of an optical storage medium |
GB2355196B (en) * | 1998-07-07 | 2004-06-09 | Coastside Bio Resources | Companion animal therapeutic treat |
AU6384099A (en) * | 1998-08-31 | 2000-03-21 | Proteotech, Inc. | Blended compositions for treatment of alzheimer's disease and other amyloidoses |
US6428817B1 (en) * | 1999-07-06 | 2002-08-06 | Peter Donald Collin | Companion animal therapeutic treat |
US6413558B1 (en) * | 1999-07-19 | 2002-07-02 | The Proctor & Gamble Co. | Compositions, kits, and methods for providing and maintaining energy and metal alertness |
US20010047032A1 (en) * | 1999-12-30 | 2001-11-29 | Castillo Gerardo M. | Polyhydroxylated aromatic compounds for the treatment of amyloidosis and alpha-synuclein fibril diseases |
US6485764B2 (en) | 2000-01-25 | 2002-11-26 | Robert A. Robergs | Hydrating beverages and method |
US6287611B1 (en) | 2000-02-01 | 2001-09-11 | Stokely-Van Camp, Inc. | Beverage having L-ascorbic acid with stability of color and clarity |
US6375992B1 (en) | 2000-02-23 | 2002-04-23 | The Procter & Gamble Co. | Methods of hydrating mammalian skin comprising oral administration of a defined composition |
US6627244B2 (en) * | 2000-04-27 | 2003-09-30 | Jinseido Company, Limited | Green tea composition and molding matter thereof, and process for producing them |
US20070208087A1 (en) | 2001-11-02 | 2007-09-06 | Sanders Virginia J | Compounds, compositions and methods for the treatment of inflammatory diseases |
CN1217583C (en) * | 2000-11-17 | 2005-09-07 | 花王株式会社 | Packaged beverages |
US20020151506A1 (en) * | 2000-12-29 | 2002-10-17 | Castillo Gerardo M. | Catechins for the treatment of fibrillogenesis in Alzheimer's disease, Parkinson's disease, systemic AA amyloidosis, and other amyloid disorders |
US20020176881A1 (en) * | 2001-01-26 | 2002-11-28 | George Verlaan | Rehydration composition |
US20020187219A1 (en) * | 2001-03-29 | 2002-12-12 | The Procter & Gamble Co. | Low glycemic response compositions |
JP3403400B1 (en) * | 2001-09-28 | 2003-05-06 | 花王株式会社 | Packaged beverage |
AUPS183302A0 (en) * | 2002-04-09 | 2002-05-30 | Belair Biotechnology Pty Ltd | Manufactured mineral water composition |
US20090022852A1 (en) * | 2002-06-21 | 2009-01-22 | Dnp Canada Inc. | Liquid Compositions Comprising Non-Digestible Oligosaccharides and Green Tea Catechins |
WO2004000045A2 (en) * | 2002-06-21 | 2003-12-31 | Canacure Corporation | Liquid compositions comprising non-digestible oligosaccharides and green tea catechins, method and uses thereof |
BR0203591A (en) * | 2002-09-05 | 2004-05-25 | Marc Kipfer | Natural rehydrating and energy drink based on coconut water, fruit juices and incorporated nutritional components |
WO2004033448A2 (en) * | 2002-10-11 | 2004-04-22 | Proteotech, Inc. | Isolation, purification and synthesis of procyanidin b2 and uses thereof |
JP3569276B2 (en) * | 2003-02-04 | 2004-09-22 | 花王株式会社 | Containerized beverage and method for producing the same |
US7160565B2 (en) * | 2003-03-31 | 2007-01-09 | Breakthru Products, Llc | Hydration beverage and method of delivering nutrients |
JP4350415B2 (en) * | 2003-05-07 | 2009-10-21 | 高砂香料工業株式会社 | Flavor composition for food and drink using green tea or oolong tea |
JP2007521010A (en) * | 2003-07-03 | 2007-08-02 | ザ プロクター アンド ギャンブル カンパニー | A composition containing green tea catechins and one or more polyvalent mineral cations |
JP3590051B1 (en) * | 2003-07-30 | 2004-11-17 | 花王株式会社 | Packaged beverage |
EP1657985A1 (en) * | 2003-08-25 | 2006-05-24 | Cargill Inc. | Beverage compositions comprising monatin and methods of making same |
US7220444B2 (en) * | 2003-09-26 | 2007-05-22 | Kao Corporation | Packaged beverages |
US20050100637A1 (en) * | 2003-11-12 | 2005-05-12 | Robert Murray | Carbohydrate and electrolyte replacement composition |
JP3766670B2 (en) * | 2003-12-16 | 2006-04-12 | 花王株式会社 | Container drink |
US20070092624A1 (en) * | 2003-12-18 | 2007-04-26 | Kao Corporation | Bottled beverage |
EP1695630B1 (en) * | 2003-12-18 | 2011-06-22 | Kao Corporation | Bottled beverage |
US20050158431A1 (en) * | 2004-01-21 | 2005-07-21 | Danisco A/S | Stabilization of cochineal dye in aqueous solutions |
US20050276839A1 (en) * | 2004-06-10 | 2005-12-15 | Rifkin Calman H | Appetite satiation and hydration beverage |
US20060062886A1 (en) * | 2004-09-22 | 2006-03-23 | Brian Takeda | Instant tea powder |
US20060099318A1 (en) * | 2004-11-04 | 2006-05-11 | Kao Corporation | Non-tea-based, packaged beverages |
JP3742094B1 (en) * | 2004-11-04 | 2006-02-01 | 花王株式会社 | Non-tea based beverage |
JP3742096B1 (en) * | 2005-02-08 | 2006-02-01 | 花王株式会社 | Non-tea based beverage |
US20060134301A1 (en) * | 2004-12-22 | 2006-06-22 | Unilever Bestfoods, North America, Division Of Conopco, Inc. | Method for making a food composition with a preservative free enhancer and a food composition |
US20060172016A1 (en) * | 2005-02-02 | 2006-08-03 | Vsevolod Kohutiak | Muscle cramp reliever |
DE102005017613A1 (en) * | 2005-04-15 | 2006-10-19 | Keme Food Engineering Ag | Instant food product or beverage has powder product applied to sweetener crystals especially sugar and pressed into single dose blocks |
US20060286223A1 (en) * | 2005-06-15 | 2006-12-21 | Carol Long | Reduced sugar RTE cereals with maltodextrin |
US20070009641A1 (en) * | 2005-07-08 | 2007-01-11 | Erickson Ken R | Stable tea concentrates |
US20070116823A1 (en) | 2005-11-23 | 2007-05-24 | The Coca-Cola Company | High-potency sweetener for hydration and sweetened hydration composition |
US7566463B2 (en) * | 2006-05-03 | 2009-07-28 | C. B. Fleet Company | Oral rehydration compositions |
US9314048B2 (en) | 2007-03-14 | 2016-04-19 | The Concentrate Manufacturing Company Of Ireland | Beverage products with non-nutritive sweetener and bitterant |
US8029846B2 (en) | 2007-03-14 | 2011-10-04 | The Concentrate Manufacturing Company Of Ireland | Beverage products |
US20080226789A1 (en) * | 2007-03-14 | 2008-09-18 | Concentrate Manufacturing Company Of Ireland | Beverage products with non-nutritive sweetener and bitterant |
US8277861B2 (en) | 2007-03-14 | 2012-10-02 | Concentrate Manufacturing Company Of Ireland | Beverage products having steviol glycosides and at least one acid |
US8277862B2 (en) | 2007-03-14 | 2012-10-02 | Concentrate Manufacturing Company Of Ireland | Beverage products having steviol glycosides and at least one acid |
US9877500B2 (en) | 2007-03-14 | 2018-01-30 | Concentrate Manufacturing Company Of Ireland | Natural beverage products |
US8084073B2 (en) | 2007-03-14 | 2011-12-27 | Concentrate Manufacturing Company Of Ireland | Anisic acid modified steviol glycoside sweetened beverage products |
US20080226790A1 (en) * | 2007-03-14 | 2008-09-18 | Concentrate Manufacturing Company Of Ireland | Long chain fatty acids for reducing off-taste of non-nutritive sweeteners |
WO2009003832A2 (en) * | 2007-07-05 | 2009-01-08 | Unilever N.V. | Composition comprising polyphenol |
WO2009003798A1 (en) * | 2007-07-05 | 2009-01-08 | Unilever N.V. | Food composition comprising trans-resveratrol and its use to control blood pressure |
WO2009003838A2 (en) * | 2007-07-05 | 2009-01-08 | Unilever N.V. | Composition comprising polyphenol |
US20090162484A1 (en) * | 2007-12-21 | 2009-06-25 | The Concentrate Manufacturing Company Of Ireland | Beverage having a non-sweetening amount of a potent natural sweetener |
WO2009150008A1 (en) * | 2008-06-10 | 2009-12-17 | Unilever Nv | Process for preparing a tea beverage |
US8435590B2 (en) * | 2008-11-24 | 2013-05-07 | Stokely-Van Camp, Inc. | Use of novel carbohydrates and carbohydrate blends to provide a sports beverage with increased absorption |
US8293299B2 (en) | 2009-09-11 | 2012-10-23 | Kraft Foods Global Brands Llc | Containers and methods for dispensing multiple doses of a concentrated liquid, and shelf stable Concentrated liquids |
JP5547939B2 (en) * | 2009-09-29 | 2014-07-16 | 花王株式会社 | Container drink |
US20110123700A1 (en) * | 2009-11-25 | 2011-05-26 | Peththawadu Pasan Thijee | Instant liquid tea concentrate |
TR201908001T4 (en) | 2010-05-11 | 2019-06-21 | The State Of Queensland | Plant-based electrolytic compositions. |
US20120171184A1 (en) | 2010-12-31 | 2012-07-05 | Lajos Szente | Cellular hydration compositions |
EP4124245A1 (en) | 2011-12-19 | 2023-02-01 | The Coca-Cola Company | Beverage comprising rebaudioside x |
US11013248B2 (en) | 2012-05-25 | 2021-05-25 | Kraft Foods Group Brands Llc | Shelf stable, concentrated, liquid flavorings and methods of preparing beverages with the concentrated liquid flavorings |
MX2015007522A (en) | 2012-12-19 | 2016-03-01 | Coca Cola Co | Compositions and methods for improving rebaudioside x solubility. |
JP5695688B2 (en) * | 2013-03-08 | 2015-04-08 | サントリー食品インターナショナル株式会社 | Beverage |
US20140272068A1 (en) | 2013-03-14 | 2014-09-18 | Indra Prakash | Beverages containing rare sugars |
MX358413B (en) | 2013-03-15 | 2018-08-20 | Coca Cola Co | Steviol glycosides, their compositions and their purification. |
US20160029677A1 (en) | 2013-03-15 | 2016-02-04 | The Coca-Cola Company | Novel glucosyl steviol glycosides, their compositions and their purification |
US10905146B2 (en) | 2013-07-12 | 2021-02-02 | The Coca-Cola Company | Compositions for improving rebaudioside M solubility |
CN106795523B (en) | 2014-08-19 | 2021-11-26 | 谱赛科有限责任公司 | Method for preparing rebaudioside I and application |
CN107072237B (en) | 2014-09-02 | 2021-12-14 | 谱赛科有限责任公司 | Stevia extract |
WO2017035527A1 (en) | 2015-08-27 | 2017-03-02 | Purecircle Sdn Bhd | Stevia extracts |
US11584769B2 (en) | 2014-11-29 | 2023-02-21 | The Coca-Cola Company | Diterpene glycosides, compositions and purification methods |
WO2016187559A1 (en) | 2015-05-20 | 2016-11-24 | Cargill, Incorporated | Glycoside compositions |
JP6779287B2 (en) | 2015-10-02 | 2020-11-04 | ザ コカ・コーラ カンパニーThe Coca‐Cola Company | Steviol glycoside sweetener with improved flavor profile |
EP3436151A4 (en) | 2016-03-28 | 2019-11-20 | The Coca-Cola Company | Sweetness and taste improvement of steviol glycoside or mogroside sweeteners with flavonoids |
CN109219355B (en) | 2016-04-06 | 2023-03-07 | 可口可乐公司 | Sweetness and taste improvement of steviol glycoside or mogroside sweeteners |
WO2018067683A1 (en) | 2016-10-04 | 2018-04-12 | The Coca-Cola Company | Diterpene glycosides containing an ent-atisene core, compositions and methods |
CN110022691A (en) | 2016-10-20 | 2019-07-16 | 可口可乐公司 | Diterpene glucoside, composition and the method separated from STEVIA REBAUDIANA |
CN110475484B (en) | 2016-12-01 | 2023-08-04 | 谱赛科美国股份有限公司 | Stevia plant and application thereof |
CA3061045A1 (en) | 2017-04-25 | 2018-11-01 | The Coca-Cola Company | Sweetness and taste improvement of steviol glycoside and mogroside sweeteners with dihydrochalcones |
CN111295101B (en) | 2017-06-27 | 2023-09-01 | 可口可乐公司 | Oral sweetener compositions and methods |
CN111356373A (en) | 2017-10-06 | 2020-06-30 | 嘉吉公司 | Organoleptic modifier compounds |
EP4342305A3 (en) | 2018-04-30 | 2024-07-24 | The Coca-Cola Company | Methods for improving the solubility of steviol glycoside mixtures, and uses |
EP4223146A1 (en) | 2018-05-08 | 2023-08-09 | EPC Natural Products Co., Ltd. | Sweetener and flavor compositions, methods of making and methods of use thereof |
CN108893215B (en) * | 2018-07-25 | 2021-05-11 | 青岛啤酒股份有限公司 | Alcohol-free beer for reducing satiety after being drunk by human body and preparation method thereof |
CN112804881A (en) * | 2018-10-05 | 2021-05-14 | 宝酒造株式会社 | Beverage containing green tea, method for suppressing fading of beverage containing green tea, and method for producing beverage containing green tea |
WO2020123067A2 (en) | 2018-10-12 | 2020-06-18 | Epc Natural Products Co., Ltd. | Sweetener and flavor compositions, methods of making and methods of use thereof |
BR112021019811A2 (en) | 2019-04-06 | 2021-12-07 | Cargill Inc | Steviol glycoside composition, beverage, methods for reducing an undesirable sensory attribute of an aqueous steviol glycoside solution, for reducing the persistence of sweetness of a steviol glycoside component in an edible composition, and for reducing the bitterness of a steviol glycoside component. steviol glycoside in an edible composition, and, aqueous solutions of steviol glycoside with reduced persistence of sweetness and aqueous solutions of steviol glycoside with reduced bitterness |
EP4033915A4 (en) | 2019-09-27 | 2023-05-31 | The Coca-Cola Company | Sweetener blends with improved taste |
Family Cites Families (35)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
DE1767652B2 (en) * | 1967-06-07 | 1977-07-28 | Stokely-Van Camp, Inc., Indianapolis, Ind. (V.St.A.) | PHYSIOLOGICALLY EFFECTIVE SOFT DRINK |
US3657424A (en) * | 1970-04-01 | 1972-04-18 | Florida State | Full-flavored citrus juice energy supplement |
GB1262235A (en) * | 1970-09-03 | 1972-02-02 | Gerard Balakian | Compositions and beverages formed therefrom for replenishing body fluids and minerals lost through perspiration |
SU523687A1 (en) * | 1974-03-27 | 1976-08-05 | Ленинградский межотраслевой научно-исследовательский институт пищевой промышленности | Dry soft drink |
US3949098A (en) * | 1974-06-05 | 1976-04-06 | Nabisco, Inc. | Nutritious orange drink concentrate, process and drink resultant therefrom |
US3950547A (en) * | 1974-08-26 | 1976-04-13 | Syntex (U.S.A.) Inc. | Dietary composition and methods of preparing |
US4042684A (en) * | 1976-03-23 | 1977-08-16 | Annika Britt Kahm | Dietetic beverage |
US4322407A (en) * | 1978-12-11 | 1982-03-30 | Vitapharm Pharmaceutical Pty. Ltd. | Electrolyte drink |
AU8221482A (en) * | 1978-12-11 | 1983-10-06 | Vitapharm Pharmaceutical Proprietary Limited | Electrolyte drink powder |
US4351735A (en) * | 1978-12-19 | 1982-09-28 | R.G.B. Laboratories Inc. | Mineral enrichment composition and method of preparing same |
JPS59203481A (en) * | 1983-04-30 | 1984-11-17 | Kiichi Nagai | Health carbonated drinking water |
US4508740A (en) * | 1983-07-11 | 1985-04-02 | General Foods Corporation | Tabletted beverage composition containing dipeptide sweetener and process therefore |
US4839347A (en) * | 1984-11-29 | 1989-06-13 | Techmix, Inc. | Composition for treating dehydration |
US4874606A (en) * | 1984-12-04 | 1989-10-17 | General Foods Corp. | Rapid rehydrating beverage |
US4567054A (en) * | 1985-05-06 | 1986-01-28 | Garyx Zimmerman | Sweetener composition |
EP0202106A3 (en) * | 1985-05-13 | 1987-10-14 | George H. Clark | A beverage and method of making a beverage for the replacement of body fluids and electrolytes |
US4748033A (en) * | 1986-05-07 | 1988-05-31 | The Procter & Gamble Company | Tea concentrate having freeze thaw stability and enhanced cold water solubility |
FI89761C (en) * | 1986-10-16 | 1993-11-25 | Sinebrychoff Ab | Use of malic acid for the production of exercise drink powder |
CA1282142C (en) * | 1986-10-21 | 1991-03-26 | Sony Corporation | Method for generating offset surface data |
JPS63160567A (en) * | 1986-12-25 | 1988-07-04 | Shiraimatsu Shinyaku Kk | Health drink composition |
JP2593882B2 (en) * | 1987-08-31 | 1997-03-26 | 三井製糖株式会社 | Sports drinks for energy replenishment |
JPH01233277A (en) * | 1988-03-15 | 1989-09-19 | Mitsui Norin Kk | Stabilization of catechins in aqueous solution |
US4906480A (en) * | 1988-04-07 | 1990-03-06 | Forsyth Dental Infirmary For Children | Sweetness and flavor enhanced compositions and method of preparing such compositions |
US5236712A (en) * | 1988-07-29 | 1993-08-17 | University Of Florida | Compositions and methods for achieving improved physiological response to exercise |
US5238684A (en) * | 1988-07-29 | 1993-08-24 | University Of Florida | Compositions and methods for achieving improved physiological response to exercise |
US5147650A (en) * | 1988-07-29 | 1992-09-15 | University Of Florida | Compositions and methods for achieving improved physiological response to exercise |
US4981687A (en) * | 1988-07-29 | 1991-01-01 | University Of Florida | Compositions and methods for achieving improved physiological response to exercise |
US5089477A (en) * | 1988-07-29 | 1992-02-18 | University Of Florida | Compositions and methods for achieving improved physiological response to exercise |
US4874790A (en) * | 1988-08-15 | 1989-10-17 | Montefiore Hospital Association Of Western Pennsylvania | Method for improving the glucose metabolism of an animal having diabetic tendencies |
JPH02223519A (en) * | 1989-02-27 | 1990-09-05 | Mitsui Norin Kk | Antitoxin against bacterial exotoxin |
US4946701A (en) * | 1989-08-04 | 1990-08-07 | Procter & Gamble | Beverages |
US4935256A (en) * | 1989-10-31 | 1990-06-19 | Procter & Gamble Company | Process for making green tea solids |
DK657789D0 (en) * | 1989-12-22 | 1989-12-22 | Novo Nordisk As | IN THE NUTRITIONALLY COMPLETE, ENTERAL, DIETETIC PRODUCT |
US5114723A (en) * | 1990-02-27 | 1992-05-19 | University Of Texas System Board Of Regents | Beverage compositions for human consumption |
GB9014756D0 (en) * | 1990-07-03 | 1990-08-22 | Unilever Plc | Tea process |
-
1994
- 1994-06-03 US US08/253,646 patent/US5464619A/en not_active Expired - Lifetime
-
1995
- 1995-05-23 ES ES95919908T patent/ES2158113T3/en not_active Expired - Lifetime
- 1995-05-23 AU AU25556/95A patent/AU2555695A/en not_active Abandoned
- 1995-05-23 AT AT95919908T patent/ATE202900T1/en active
- 1995-05-23 JP JP50099796A patent/JP3620600B2/en not_active Expired - Fee Related
- 1995-05-23 CA CA002191712A patent/CA2191712C/en not_active Expired - Fee Related
- 1995-05-23 EP EP95919908A patent/EP0762836B1/en not_active Expired - Lifetime
- 1995-05-23 WO PCT/US1995/006508 patent/WO1995033385A1/en active IP Right Grant
- 1995-05-23 BR BR9507835A patent/BR9507835A/en not_active Application Discontinuation
- 1995-05-23 HU HU9603321A patent/HU9603321D0/en unknown
- 1995-05-23 PL PL95317431A patent/PL317431A1/en unknown
- 1995-05-23 CN CN95193874A patent/CN1075715C/en not_active Expired - Fee Related
- 1995-05-23 DE DE69521701T patent/DE69521701T2/en not_active Expired - Lifetime
- 1995-11-06 US US08/553,935 patent/US5681569A/en not_active Expired - Lifetime
-
1996
- 1996-12-02 NO NO965130A patent/NO965130D0/en unknown
- 1996-12-03 FI FI964836A patent/FI964836A0/en not_active Application Discontinuation
-
2001
- 2001-10-11 GR GR20010401744T patent/GR3036880T3/en unknown
Cited By (3)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US9101160B2 (en) | 2005-11-23 | 2015-08-11 | The Coca-Cola Company | Condiments with high-potency sweetener |
WO2008012147A1 (en) | 2006-07-24 | 2008-01-31 | Unilever Plc | Improved beverage |
US8017168B2 (en) | 2006-11-02 | 2011-09-13 | The Coca-Cola Company | High-potency sweetener composition with rubisco protein, rubiscolin, rubiscolin derivatives, ace inhibitory peptides, and combinations thereof, and compositions sweetened therewith |
Also Published As
Publication number | Publication date |
---|---|
DE69521701D1 (en) | 2001-08-16 |
WO1995033385A1 (en) | 1995-12-14 |
FI964836A0 (en) | 1996-12-03 |
US5464619A (en) | 1995-11-07 |
CN1151679A (en) | 1997-06-11 |
ES2158113T3 (en) | 2001-09-01 |
DE69521701T2 (en) | 2002-05-08 |
CN1075715C (en) | 2001-12-05 |
JP3620600B2 (en) | 2005-02-16 |
EP0762836A1 (en) | 1997-03-19 |
JPH10501407A (en) | 1998-02-10 |
HU9603321D0 (en) | 1997-01-28 |
GR3036880T3 (en) | 2002-01-31 |
CA2191712C (en) | 2000-02-29 |
AU2555695A (en) | 1996-01-04 |
NO965130D0 (en) | 1996-12-02 |
CA2191712A1 (en) | 1995-12-14 |
ATE202900T1 (en) | 2001-07-15 |
PL317431A1 (en) | 1997-04-14 |
BR9507835A (en) | 1997-09-02 |
US5681569A (en) | 1997-10-28 |
Similar Documents
Publication | Publication Date | Title |
---|---|---|
EP0762836B1 (en) | Beverage compositions containing green tea solids, electrolytes and carbohydrates to provide improved cellular hydration and drinkability | |
EP1633209B1 (en) | Weight management beverage | |
CA2196292C (en) | Color stable composition containing tea and fruit juice | |
US5114723A (en) | Beverage compositions for human consumption | |
US5032411A (en) | Beverage compositions for human consumption | |
US7160565B2 (en) | Hydration beverage and method of delivering nutrients | |
TWI331511B (en) | Beverage having high concentration of non-polymer catechins | |
US6723369B2 (en) | Carbonated beverage for strengthening acid resistancy of teeth | |
US20120040075A1 (en) | Package drink | |
TWI492715B (en) | Containing polymerized catechins | |
JP4542047B2 (en) | Method for producing purified green tea extract | |
US20070141219A1 (en) | Bottle beverage | |
EP2036551B1 (en) | Catechins for improving muscle power | |
US20090061016A1 (en) | Seawater Based Dietary Supplement Product for Energy and Electrolyte Replacement | |
JP4181982B2 (en) | Containerized beverage containing purified green tea extract | |
JP3615213B1 (en) | Container drink | |
US20090061050A1 (en) | Seawater based dietary supplement product for energy and electrolyte replacement | |
JPS6094075A (en) | Fruit juice drink composition | |
MXPA96006056A (en) | Drinking compositions containing solids of green tea, electrolytes and carbohydrates to provide better cellular hydration and high volume of consumption | |
KR102541973B1 (en) | Method for producing functional dutch coffee | |
MXPA05012641A (en) | Weight management beverage | |
SK284000B6 (en) | Syrup for production of drinks and process of production thereof |
Legal Events
Date | Code | Title | Description |
---|---|---|---|
PUAI | Public reference made under article 153(3) epc to a published international application that has entered the european phase |
Free format text: ORIGINAL CODE: 0009012 |
|
17P | Request for examination filed |
Effective date: 19961204 |
|
AK | Designated contracting states |
Kind code of ref document: A1 Designated state(s): AT BE CH DE DK ES FR GB GR IE IT LI LU NL PT SE |
|
17Q | First examination report despatched |
Effective date: 19990430 |
|
GRAG | Despatch of communication of intention to grant |
Free format text: ORIGINAL CODE: EPIDOS AGRA |
|
GRAG | Despatch of communication of intention to grant |
Free format text: ORIGINAL CODE: EPIDOS AGRA |
|
GRAH | Despatch of communication of intention to grant a patent |
Free format text: ORIGINAL CODE: EPIDOS IGRA |
|
GRAH | Despatch of communication of intention to grant a patent |
Free format text: ORIGINAL CODE: EPIDOS IGRA |
|
GRAA | (expected) grant |
Free format text: ORIGINAL CODE: 0009210 |
|
AK | Designated contracting states |
Kind code of ref document: B1 Designated state(s): AT BE CH DE DK ES FR GB GR IE IT LI LU NL PT SE |
|
PG25 | Lapsed in a contracting state [announced via postgrant information from national office to epo] |
Ref country code: LI Free format text: LAPSE BECAUSE OF FAILURE TO SUBMIT A TRANSLATION OF THE DESCRIPTION OR TO PAY THE FEE WITHIN THE PRESCRIBED TIME-LIMIT Effective date: 20010711 Ref country code: IT Free format text: LAPSE BECAUSE OF FAILURE TO SUBMIT A TRANSLATION OF THE DESCRIPTION OR TO PAY THE FEE WITHIN THE PRE;WARNING: LAPSES OF ITALIAN PATENTS WITH EFFECTIVE DATE BEFORE 2007 MAY HAVE OCCURRED AT ANY TIME BEFORE 2007. THE CORRECT EFFECTIVE DATE MAY BE DIFFERENT FROM THE ONE RECORDED.SCRIBED TIME-LIMIT Effective date: 20010711 Ref country code: CH Free format text: LAPSE BECAUSE OF FAILURE TO SUBMIT A TRANSLATION OF THE DESCRIPTION OR TO PAY THE FEE WITHIN THE PRESCRIBED TIME-LIMIT Effective date: 20010711 |
|
REF | Corresponds to: |
Ref document number: 202900 Country of ref document: AT Date of ref document: 20010715 Kind code of ref document: T |
|
REG | Reference to a national code |
Ref country code: CH Ref legal event code: EP |
|
REF | Corresponds to: |
Ref document number: 69521701 Country of ref document: DE Date of ref document: 20010816 |
|
REG | Reference to a national code |
Ref country code: IE Ref legal event code: FG4D |
|
REG | Reference to a national code |
Ref country code: ES Ref legal event code: FG2A Ref document number: 2158113 Country of ref document: ES Kind code of ref document: T3 |
|
PG25 | Lapsed in a contracting state [announced via postgrant information from national office to epo] |
Ref country code: SE Free format text: LAPSE BECAUSE OF FAILURE TO SUBMIT A TRANSLATION OF THE DESCRIPTION OR TO PAY THE FEE WITHIN THE PRESCRIBED TIME-LIMIT Effective date: 20011011 Ref country code: PT Free format text: LAPSE BECAUSE OF FAILURE TO SUBMIT A TRANSLATION OF THE DESCRIPTION OR TO PAY THE FEE WITHIN THE PRESCRIBED TIME-LIMIT Effective date: 20011011 Ref country code: DK Free format text: LAPSE BECAUSE OF FAILURE TO SUBMIT A TRANSLATION OF THE DESCRIPTION OR TO PAY THE FEE WITHIN THE PRESCRIBED TIME-LIMIT Effective date: 20011011 |
|
ET | Fr: translation filed | ||
REG | Reference to a national code |
Ref country code: GB Ref legal event code: IF02 |
|
REG | Reference to a national code |
Ref country code: GR Ref legal event code: EP Ref document number: 20010401744 Country of ref document: GR |
|
REG | Reference to a national code |
Ref country code: CH Ref legal event code: PL |
|
PLBE | No opposition filed within time limit |
Free format text: ORIGINAL CODE: 0009261 |
|
STAA | Information on the status of an ep patent application or granted ep patent |
Free format text: STATUS: NO OPPOSITION FILED WITHIN TIME LIMIT |
|
PG25 | Lapsed in a contracting state [announced via postgrant information from national office to epo] |
Ref country code: LU Free format text: LAPSE BECAUSE OF NON-PAYMENT OF DUE FEES Effective date: 20020523 Ref country code: IE Free format text: LAPSE BECAUSE OF NON-PAYMENT OF DUE FEES Effective date: 20020523 |
|
26N | No opposition filed | ||
REG | Reference to a national code |
Ref country code: IE Ref legal event code: MM4A |
|
PGFP | Annual fee paid to national office [announced via postgrant information from national office to epo] |
Ref country code: ES Payment date: 20120518 Year of fee payment: 18 |
|
PGFP | Annual fee paid to national office [announced via postgrant information from national office to epo] |
Ref country code: AT Payment date: 20120426 Year of fee payment: 18 |
|
PGFP | Annual fee paid to national office [announced via postgrant information from national office to epo] |
Ref country code: DE Payment date: 20130531 Year of fee payment: 19 Ref country code: GB Payment date: 20130425 Year of fee payment: 19 |
|
PGFP | Annual fee paid to national office [announced via postgrant information from national office to epo] |
Ref country code: FR Payment date: 20130531 Year of fee payment: 19 Ref country code: NL Payment date: 20130514 Year of fee payment: 19 Ref country code: GR Payment date: 20130426 Year of fee payment: 19 |
|
PGFP | Annual fee paid to national office [announced via postgrant information from national office to epo] |
Ref country code: BE Payment date: 20130604 Year of fee payment: 19 |
|
REG | Reference to a national code |
Ref country code: DE Ref legal event code: R119 Ref document number: 69521701 Country of ref document: DE |
|
REG | Reference to a national code |
Ref country code: NL Ref legal event code: V1 Effective date: 20141201 |
|
REG | Reference to a national code |
Ref country code: AT Ref legal event code: MM01 Ref document number: 202900 Country of ref document: AT Kind code of ref document: T Effective date: 20140523 |
|
GBPC | Gb: european patent ceased through non-payment of renewal fee |
Effective date: 20140523 |
|
PG25 | Lapsed in a contracting state [announced via postgrant information from national office to epo] |
Ref country code: GR Free format text: LAPSE BECAUSE OF NON-PAYMENT OF DUE FEES Effective date: 20141203 |
|
REG | Reference to a national code |
Ref country code: GR Ref legal event code: ML Ref document number: 20010401744 Country of ref document: GR Effective date: 20141203 |
|
REG | Reference to a national code |
Ref country code: DE Ref legal event code: R119 Ref document number: 69521701 Country of ref document: DE Effective date: 20141202 |
|
PG25 | Lapsed in a contracting state [announced via postgrant information from national office to epo] |
Ref country code: AT Free format text: LAPSE BECAUSE OF NON-PAYMENT OF DUE FEES Effective date: 20140523 Ref country code: NL Free format text: LAPSE BECAUSE OF NON-PAYMENT OF DUE FEES Effective date: 20141201 |
|
REG | Reference to a national code |
Ref country code: FR Ref legal event code: ST Effective date: 20150130 |
|
PG25 | Lapsed in a contracting state [announced via postgrant information from national office to epo] |
Ref country code: DE Free format text: LAPSE BECAUSE OF NON-PAYMENT OF DUE FEES Effective date: 20141202 |
|
PG25 | Lapsed in a contracting state [announced via postgrant information from national office to epo] |
Ref country code: FR Free format text: LAPSE BECAUSE OF NON-PAYMENT OF DUE FEES Effective date: 20140602 Ref country code: GB Free format text: LAPSE BECAUSE OF NON-PAYMENT OF DUE FEES Effective date: 20140523 |
|
REG | Reference to a national code |
Ref country code: ES Ref legal event code: FD2A Effective date: 20150626 |
|
PG25 | Lapsed in a contracting state [announced via postgrant information from national office to epo] |
Ref country code: ES Free format text: LAPSE BECAUSE OF NON-PAYMENT OF DUE FEES Effective date: 20140524 |
|
PG25 | Lapsed in a contracting state [announced via postgrant information from national office to epo] |
Ref country code: BE Free format text: LAPSE BECAUSE OF NON-PAYMENT OF DUE FEES Effective date: 20140531 |